Clinical management of persistent ACTH excess in Nelson´s syndrome (NS) and Cushing´s disease (CD) remains a challenge. Somatostatin (SS) and its analogs as octreotide decrease ACTH secretion through SS receptors (sst) of pituitary cells. To our knowledge there are no reports on the effect of long-acting repeatable octreotide (oct-lar) on hormonal secretion and quality of life in patients with NS and CD who failed conventional therapy. Herein we describe the effects of treatment with oct-lar (20 mg/ i.m. month) in one woman with NS and two women with persistent CD . Oct-lar therapy reduced ACTH secretion and improved quality of life in NS, by contrast in CD it failed to control ACTH and cortisol secretion and quality of life remained u...
CONTEXT: Criteria to define the response to somatostatin (SS) analogs (SSA) in acromegaly are based...
In this case report we demonstrated that treatment with the long-acting D2 receptor agonist cabergol...
Surgical cure cannot be achieved in most patients with invasive non-functioning pituitary macroadeno...
We studied a 55-year old woman presenting with features of Cushing's syndrome associated with metabo...
Abstract Cushing's disease: Excessive corticotroph hormone levels sustained by an adrenocorticotropi...
The effect of somatostatin on thyroid function was studied in 12 patients with growth hormone (GH)-s...
textabstractContext: Corticotroph pituitary adenomas often highly express the dopamine 2 receptor (D...
Pasireotide is the first pituitary-directed drug approved for treating patients with Cushing's disea...
Cushing's disease is caused by an ACTH secreting pituitary adenoma. Surgery is the treatment of choi...
Objective: Currently, there is no effective medical treatment for patients with pituitary-dependent ...
Purpose: Cushing’s disease (CD) is associated with significant clinical burden, increased mortality ...
Abstract Background Nelson’s syndrome is a well-descr...
The effects of a 12- to 24-month treatment with depot long-acting octreotide (OCT-LAR) on hormone pr...
PURPOSE: Nelson's syndrome is a challenging condition that can develop following bilateral adrenalec...
As described originally, Nelson's syndrome is characterized by grossly elevated ACTH concentrations,...
CONTEXT: Criteria to define the response to somatostatin (SS) analogs (SSA) in acromegaly are based...
In this case report we demonstrated that treatment with the long-acting D2 receptor agonist cabergol...
Surgical cure cannot be achieved in most patients with invasive non-functioning pituitary macroadeno...
We studied a 55-year old woman presenting with features of Cushing's syndrome associated with metabo...
Abstract Cushing's disease: Excessive corticotroph hormone levels sustained by an adrenocorticotropi...
The effect of somatostatin on thyroid function was studied in 12 patients with growth hormone (GH)-s...
textabstractContext: Corticotroph pituitary adenomas often highly express the dopamine 2 receptor (D...
Pasireotide is the first pituitary-directed drug approved for treating patients with Cushing's disea...
Cushing's disease is caused by an ACTH secreting pituitary adenoma. Surgery is the treatment of choi...
Objective: Currently, there is no effective medical treatment for patients with pituitary-dependent ...
Purpose: Cushing’s disease (CD) is associated with significant clinical burden, increased mortality ...
Abstract Background Nelson’s syndrome is a well-descr...
The effects of a 12- to 24-month treatment with depot long-acting octreotide (OCT-LAR) on hormone pr...
PURPOSE: Nelson's syndrome is a challenging condition that can develop following bilateral adrenalec...
As described originally, Nelson's syndrome is characterized by grossly elevated ACTH concentrations,...
CONTEXT: Criteria to define the response to somatostatin (SS) analogs (SSA) in acromegaly are based...
In this case report we demonstrated that treatment with the long-acting D2 receptor agonist cabergol...
Surgical cure cannot be achieved in most patients with invasive non-functioning pituitary macroadeno...